Convert to ICD-10-CM:
270.0 converts approximately to:
- 2015/16 ICD-10-CM E72.00 Disorders of amino-acid transport, unspecified
Or:
- 2015/16 ICD-10-CM E72.01 Cystinuria
Or:
- 2015/16 ICD-10-CM E72.04 Cystinosis
Or:
- 2015/16 ICD-10-CM E72.09 Other disorders of amino-acid transport
ICD-9-CM Volume 2 Index entries containing back-references to
270.0:
- Abderhalden-Kaufmann-Lignac syndrome (cystinosis) 270.0
- Beta-mercaptolactate-cysteine disulfiduria 270.0
- Blue
- diaper syndrome 270.0
- Cystinosis (malignant) 270.0
- Cystinuria 270.0
- Deficiency, deficient
- sulfite oxidase 270.0
- de Toni-Fanconi syndrome (cystinosis) 270.0
- Diathesis
- cystine (familial) 270.0
- Disease, diseased - see also Syndrome
- cystine storage (with renal sclerosis) 270.0
- H 270.0
- Hart's (pellagra-cerebellar ataxia-renal aminoaciduria) 270.0
- Hartnup (pellagra-cerebellar ataxia-renal aminoaciduria) 270.0
- Lignac's (cystinosis) 270.0
- Disorder - see also Disease
- amino acid (metabolic) (see also Disturbance, metabolism, amino acid) 270.9
- albinism 270.2
- alkaptonuria 270.2
- argininosuccinicaciduria 270.6
- beta-amino-isobutyricaciduria 277.2
- cystathioninuria 270.4
- cystinosis 270.0
- cystinuria 270.0
- glycinuria 270.0
- homocystinuria 270.4
- imidazole 270.5
- maple syrup (urine) disease 270.3
- neonatal, transitory 775.89
- oasthouse urine disease 270.2
- ochronosis 270.2
- phenylketonuria 270.1
- phenylpyruvic oligophrenia 270.1
- purine NEC 277.2
- pyrimidine NEC 277.2
- renal transport NEC 270.0
- specified type NEC 270.8
- transport NEC 270.0
- xanthinuria 277.2
- Disturbance - see also Disease
- amino acid (metabolic) (see also Disorder, amino acid) 270.9
- imidazole 270.5
- maple syrup (urine) disease 270.3
- transport 270.0
- metabolism (acquired) (congenital) (see also Disorder, metabolism) 277.9
- Disulfiduria, beta-mercaptolactate-cysteine 270.0
- Dwarf, dwarfism 259.4
- nephrotic-glycosuric, with hypophosphatemic rickets 270.0
- Fanconi (-de Toni) (-Debré) syndrome (cystinosis) 270.0
- Glycinuria (renal) (with ketosis) 270.0
- Hart's disease or syndrome (pellagra-cerebellar ataxia-renal aminoaciduria) 270.0
- Hartnup disease (pellagra-cerebellar ataxia-renal aminoaciduria) 270.0
- H disease 270.0
- Hyperaminoaciduria 270.9
- cystine 270.0
- glycine 270.0
- renal (types I, II, III) 270.0
- Lignac's disease (cystinosis) 270.0
- Lignac (-de Toni) (-Fanconi) (-Debré) syndrome (cystinosis) 270.0
- Lignac (-Fanconi) syndrome (cystinosis) 270.0
- Pellagra-cerebellar-ataxia-renal aminoaciduria syndrome 270.0
- Rickets (active) (acute) (adolescent) (adult) (chest wall) (congenital) (current) (infantile) (intestinal) 268.0
- hypophosphatemic with nephrotic-glycosuric dwarfism 270.0
- Sclerosis, sclerotic
- renal 587
- with
- cystine storage disease 270.0
- hypertension (see also Hypertension, kidney) 403.90
- hypertensive heart disease (conditions classifiable to 402) (see also Hypertension, cardiorenal) 404.90
- arteriolar (hyaline) (see also Hypertension, kidney) 403.90
- hyperplastic (see also Hypertension, kidney) 403.90
- Stone(s) - see also Calculus
- cystine 270.0
- Syndrome - see also Disease
- blue
- de Toni-Fanconi (-Debre) (cystinosis) 270.0
- Fanconi (-de Toni) (-Debré) (cystinosis) 270.0
- Hart's (pellagra-cerebellar ataxia-renal aminoaciduria) 270.0
- Lignac (-de Toni) (-Fanconi) (-Debré) (cystinosis) 270.0
- pellagra-cerebellar ataxia-renal aminoaciduria 270.0
- Toni-Fanconi (cystinosis) 270.0
- Thesaurismosis
- cystine 270.0
- Toni-Fanconi syndrome (cystinosis) 270.0